GEO Accession viewer

GSE14867	SNP/CNV analysis in a breast cancer metastasis model
GSE15096	Affymetrix SNP 6.0 array data for human embryonic stem cell lines
GSE15097	High resolution genome wide DNA analysis on a large panel of Human Embryonic stem cell lines
GSE15264	TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma
GSE15619	Epigenetic signature of breast cancer and its association with gene expression and copy number
GSE15688	Acquired mutations in TET2 are common in myelodysplastic syndromes
GSE15826	Affymetrix 6.0 study of sporadic motor neuron disease patients and controls.
GSE17359	Affymetrix SNP array data for melanoma short-term cultures and cell lines
GSE17593	Melanoma short-term cultures and cell lines: expression profiling and CNV analyses
GSE18333	Distinct genomic differences in prostate cancer between Western countries and China
GSE18642	Definitive SNP/CNV haplotype map of Asians determined using a collection of complete hydatidiform moles (Affymetrix)
GSE18701	Definitive SNP/CNV haplotype map of Asians determined using a collection of complete hydatidiform moles
GSE18828	Affymetrix SNP array data for Diffuse Intrinsic Pontine Glioma
GSE19416	Genome-wide copy number variation in TP53 mutation negative ovarian tumours
GSE19539	Identification of Novel Oncogene Loci in Ovarian Cancer through Integrated Copy Number and Expression Analysis
GSE19949	Integrative genome-wide expression profiling identifies three distinct molecular subgroups of renal cell carcinoma with different patient outcome
GSE20206	Acquired chromosome abnormalities in the lungs of patients with Pulmonary Arterial Hypertension
GSE20275	Affymetrix SNP and CNV data for the HuRef individual
GSE20290	Towards a comprehensive structural variation map of an individual human genome for personalized medicine
GSE20533	Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
GSE20564	Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13
GSE20565	Primary and secondary ovarian tumors
GSE20584	Affymetrix SNP6.0 array for comparison of lung tumor and adjacent normal to high-throughput sequencing data
GSE20585	The mutation spectrum revealed by paired genome sequences from a lung cancer patient
GSE20672	Identification of novel sub-microscopic copy number aberrations in adult acute myeloid leukemia
GSE20709	Copy number data from GIST with KIT mutation
GSE20710	Integrative analysis of gene expression profiling and genomic copy number in Gastrointestinal Stromal Tumors
GSE21107	NF1 inactivation in adult acute myelogenous leukemia
GSE21228	Identification of SNP candidates associated with chemo-responsiveness in colorectal cancer patients
GSE21661	Affymetrix SNP array data for 31 Tibetan samples
GSE21780	SNP arrays in matched diagnosis/remission samples of normal karyotype-acute myeloid leukemia
GSE21990	Affymetrix SNP 6.0 array data for myelodysplastic/myeloproliferative neoplasms
GSE21991	Myelodysplastic/myeloproliferative neoplasms
GSE22208	Integrative analysis reveals selective 9p24.1 amplification, increased PD-1 ligand expression, and further induction via JAK2 in nodular sclerosing Hodgkin lymphoma and primary mediastinal large B-cell lymphoma
GSE22305	Clinical relevance of SKP2 alterations in metastatic melanoma
GSE22306	Integrative genomics identifies molecular alterations that differentiate superficial spreading and nodular melanoma
GSE22461	Affymetrix copy number data for melanoma cell line mapping
GSE22615	Genomic alterations of chromosome 11 induce transcriptomic dysregulation in aggressive and malignant prolactin tumours
GSE22928	Genome-Wide Analysis of Somatic Copy Number Alterations (CGH, SNP) and Gene Expression (RNA-seq) in Metastatic Melanoma
GSE22965	Genome-wide analysis of Ollier disease: Is it all in the genes?
GSE22984	Affymetrix SNP6.0 on Ollier disease-related tumors
GSE23056	Genome-Wide Analysis of Somatic Copy Number Alterations and Gene Expression in Metastatic Melanoma
GSE23201	Large rare Deletions in Ashkenazi Jewish schizophrenia cases vs controls
GSE23300	Affymetrix SNP6.0 microarray data - Myelodysplastic syndromes
GSE23358	Intellectual disability and mood disorder associated with partial deletion of the Neurexin 1 Gene
GSE23414	Reprogramming of Human Fibroblasts into Hematopoietic Progenitors by Fusion With Human Fetal Liver CD34+ Cells (GenomeWideSNP_6)
GSE23416	Reprogramming of Human Fibroblasts into Hematopoietic Progenitors by Fusion With Human Fetal Liver CD34+ Cells
GSE23452	Acquired Genomic Copy Number Aberrations and Survival in Adult Acute Myelogenous Leukemia
GSE23557	Genotyping data from 49 patient with unexplained mental retardation
GSE23587	Homologous recombination between nonhomologous chromosomes – Recurrent chromosomal translocations mediated by interchromosomal NAHR
GSE23636	Population genetic structure of the Ashkenazi Jewish population
GSE24144	Affymetrix SNP array data for EZH2 mediated gene copy number change in breast tumor initiating cells
GSE24546	Evaluation of affinity-based genome-wide DNA methylation data: effects of CpG density, amplification bias and copy number variation
GSE24947	Genome-wide connection between DNA methylation and DNA replication timing
GSE25016	Frequent and Focal FGFR1 Amplification Associates With Therapeutically Tractable FGFR1 Dependency in Squamous-cell Lung Cancer.
GSE25103	Affymetrix SNP array data for oral squamous cell carcinoma
GSE25104	Expression and SNP array data for oral squamous cell carcinoma
GSE25262	Genetic adaptability of cancer cells under treatment selection pressure in multiple myeloma patients.
GSE25492	Copy number analysis of spontaneously transformed hTERT-immortalized ovarian surface epithelial cells
GSE25540	DNA Copy-Number Alterations in clear-cell Renal Cell Carcinoma (ccRCC) Tumors and Tumorgrafts for samples deficient in BAP1 or PBRM1
GSE25720	Affymetrix SNP 6.0 array data for chordoma samples
GSE25839	Affymetrix SNP array data for Primary Effusion Lymphoma samples
GSE25893	A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
GSE25989	Copy number analysis of Hodgkin lymphoma cell lines KM-H2 and L-428
GSE25990	Hodgkin lymphoma
GSE26034	Affymetrix SNP6.0 array data for different clinical outcomes of HBV infection
GSE26053	Tissue samples from the same individual patient
GSE26173	Affymetrix SNP6.0 data for human induced pluripotent stem cells (hiPSCs), human Fibroblasts, and human embryonic stem cells (hESCs)
GSE26232	Genomic profiles vary with race and subtype in young African American and European American breast cancer (SNP)
GSE26233	Genomic profiles vary with race and subtype in young African American and European American breast cancer
GSE26301	Affymetrix SNP array data for ovarian cancer cells OVCAR-3 and FU-OV-1
GSE26302	Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity
GSE26576	Genome-wide Analyses of Diffuse Intrinsic Pontine Gliomas
GSE26674	SNP array analysis on Maffucci tumours
GSE26675	Maffucci tumours
GSE26853	SNP data from blood DNAs of patients with gastric cancer
GSE26860	ENPP1 deletion and infantile arterial calcification
GSE27105	Genomic Signatures of Metastasis in Prostate Cancer
GSE27135	Affymetrix SNP array data for different passages of mesenchymal stem cells.
GSE27145	Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR (GenomeWideSNP_6)
GSE27367	Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR
GSE27560	Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients
GSE27692	Molecular profiles for GTL16 cell lines
GSE27832	CDKN1B encoding the cyclin-dependent kinase inhibitor 1B (p27) is located in the minimally deleted region of 12p abnormalities in myeloid malignancies and its low expression is a favorable prognostic marker in acute myeloid leukemia
GSE28111	A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6)
GSE28132	Affymetrix SNP 6.0 array data for single cell multiple displacement amplification
GSE28910	Genome wide analysis of acral melanoma (Affymetrix)
GSE28913	Genome wide analysis of acral melanoma
GSE29062	Orthotopic xenografts of RCC retain histological, immunophenotypic and genetic features of tumors in patients
GSE29172	SNP array analysis of lung cancer NCI-H1395, diluted to different tumor cell concentrations
GSE29283	Pediatric Hepatocellular Carcinoma Celll Line
GSE29569	High-resolution genome-wide copy-number analysis suggests a monoclonal origin of multi-focal prostate cancer
GSE29667	Affymetrix SNP array data for hepatocellular carcinoma tissue
GSE29772	CNV analysis for Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
GSE29774	Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
GSE29851	Genetic analysis of ancestry, admixture, and selection in Bolivian and Totonac populations of the New World
GSE29876	Assessment of palindromes as platforms for DNA amplification in breast cancer
GSE29996	Deep sequencing of gastric carcinoma reveals somatic mutations relevant to personalized medicine [Affymetrix SNP array data]
GSE29999	Deep sequencing of gastric carcinoma reveals somatic mutations relevant to personalized medicine
GSE30182	COLO320 DNA copy number analysis
GSE30283	The histotype-specific copy-number landscape of ovarian cancer (copy number Japan)
GSE30300	The histotype-specific copy-number landscape of ovarian cancer (copy number SNP)
GSE30311	The histotype-specific copy-number landscape of ovarian cancer
GSE30348	Dominant MLH1 epimutation linked to 5'UTR variant c.-27C>A
GSE30475	Colorectal Cancer Cells
GSE30481	A Map of Copy Number Variations in Chinese Populations
GSE30777	Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia
GSE31168	Genetic Landscape of Copy Number Alterations in Gastric Cancer
GSE31272	NF-kB activation confers a prolonged event-free-survival in newly diagnosed myeloma patients harboring t(4;14) treated with bortezomib.
GSE31276	Genetic Copy Number Variants in Myocardial Infarction Patients with Hyperlipidemia
GSE31339	Affymetrix SNP array data for Monoclonal Gammopathies samples
GSE32191	Genomic alterations of chromosome 11 induce transcriptome dysregulation in aggressive and malignant prolactin tumours
GSE32258	Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers [SNP data]
GSE32259	Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers
GSE32462	High-Resolution Genomic Profiling of Adult and Pediatric Core-Binding-Factor Acute Myeloid Leukemia Reveals New Recurrent Genomic Alterations
GSE32530	Primary tumor grafts as advanced models for breast cancer that authentically reflect tumor histopathology, growth, metastasis, and patient outcomes (copy number)
GSE32532	Patient-derived tumor grafts authentically reflect tumor pathology, growth, metastasis, and disease outcomes
GSE32682	Integrative Survival-Based Molecular Profiling of Human Pancreatic Cancer [SNP]
GSE32688	Integrative Survival-Based Molecular Profiling of Human Pancreatic Cancer
GSE33032	Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood
GSE33153	Copy number analysis of high-grade osteosarcoma
GSE33229	Cancer Outlier Gene Profile Sets Elucidate Pathways and Patient-Specific Targets in Head and Neck Squamous Cell Carcinoma [Affymetrix SNP6]
GSE33232	Cancer Outlier Gene Profile Sets Elucidate Pathways and Patient-Specific Targets in Head and Neck Squamous Cell Carcinoma
GSE33355	Affymetrix SNP array data for Non-Smoking Female Lung Cancer in Taiwan
GSE33356	Genome-wide screening of genomic alterations and transcriptional modulation in non-smoking female lung cancer in Taiwan
GSE33383	Identification of osteosarcoma driver genes by integrative analysis of copy number and gene expression data
GSE33598	Genomic exploration of monozygotic twins discordant (MZD) for schizophrenia uncovers de novo mutations (DNM) and reveals candidate genes
GSE33733	Complete OATP1B1 and OATP1B3 deficiency underlies human Rotor syndrome.
GSE33848	MERLION LUNG CANCER STUDY_2_DNA
GSE34171	Integrative Analysis of a series of newly diagnosed Diffuse Large B-cell Lymphomas (DLBCLs)
GSE34211	Pfizer Molecular Profile Data for Cell Lines
GSE34258	Genome sequencing of childhood medulloblastoma brain tumors links chromothripsis with TP53 mutations
GSE34280	Clonal Selection Drives Genetic Divergence of Metastatic Medulloblastoma [Affymetrix SNP6 Arrays]
GSE34323	Genome wide analysis of tumours in individuals with p53-germline mutations
GSE34356	Clonal Selection Drives Genetic Divergence of Metastatic Medulloblastoma
GSE34542	Affymetrix SNP array data for acute myeloid leukemia (AML) samples with complex karyotype
GSE34676	Renal Cell Neoplasms Contain Shared Tumor Type-Specific Copy Number Variations
GSE35282	SNP data from genomic DNA in patient with rectal cancer
GSE35656	Affymetrix SNP array data for myelodysplastic syndrome with 5q deletion treated with lenalidomide
GSE35991	Affymetrix SNP array data for a melanoma lesion and a cellline derived thereof
GSE36003	Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma [DNA copy number]
GSE36004	Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma.
GSE36311	High-resolution genomic profiling of marginal zone B-cell lymphomas and variants
GSE36363	Human lung adenocarcinoma DNA copy number profiling
GSE36458	Affymetrix SNP 6.0 array data for colon, gastric and esophageal adenocarcinoma cancer types
GSE36460	Gastrointestinal Adenocarcinomas of the Esophagus, Stomach, and Colon Exhibit Distinct Patterns of Genome Instability and Oncogenesis.
GSE36471	Human lung adenocarcinoma
GSE36790	Cetuximab resistant or sensitive head and neck cancer samples
GSE36908	High-Resolution Genomic Profiling of Chronic Lymphocytic Leukemia Reveals New Recurrent Genomic Alterations
GSE36950	SNP array for CNV calling AUTS2 project [Affymetrix]
GSE36967	Affymetrix SNP 6.0 profiles of 10 Human B-NHL lines
GSE37035	Polarity gene alterations in pure invasive micropapillary carcinomas of the breast
GSE37259	Gene copy number variations associated with patient survival in uveal melanoma
GSE37384	Subgroup specific somatic copy number aberrations in the medulloblastoma genome [gDNA]
GSE37385	Subgroup specific somatic copy number aberrations in the medulloblastoma genome
GSE37469	Minor clone provides a reservoir for relapse in multiple myeloma
GSE37657	AUTS2 project
GSE37977	SNP6.0 copy number analysis of eight diffuse large B-cell samples and one matched blood sample
GSE37979	Performance Comparison of the Affymetrix SNP6.0 and Cytogenetic 2.7M Whole-genome Microarrays in Complex Cancer Samples
GSE38073	DNA methylation profiling of normal prostates and prostate cancer metastases [Affymetrix]
GSE38149	Copy Number Variants at Chromosome 10q11.21, 12p12.1 and 21q22.11 May Be Associated with Hyperlipidemia in Taiwanese Patients
GSE38242	DNA methylation alterations exhibit striking intra-individual stability and inter-individual heterogeneity across metastatic dissemination
GSE38548	Somatic cell fusions reveal extensive heterogeneity in basal-like breast cancer
GSE38787	Copy number data from paired primary and relapse ovarian tumours
GSE39076	High-resolution genome-wide copy number analysis of pre-invasive mucinous ovarian tumours
GSE39367	Molecular Subtypes in Head and Neck Cancer [copy number]
GSE39368	Molecular Subtypes in Head and Neck Cancer
GSE39371	Affymetrix SNP 6.0 array data from neuroendocrine primary tumor and its metastasis
GSE39412	Somatic cell fusions reveal extensive heterogeneity in basal-like breast cancer [SNP]
GSE40142	A framework for identification of actionable cancer genome dependencies in small cell lung cancer
GSE40546	CTCR-OV03/CTCR-OV04 ovarian cancer
GSE40769	Comparison of Cancer-Associated Genetic Abnormalities in Columnar-Lined Esophagus with and without Goblet Cells
GSE41308	Affymetrix SNP6 array data for 56 breast cancer cell lines
GSE41646	Clonal evolution and devolution following chemotherapy in adult acute myelogenous leukemia
GSE42040	Diverse phospho-signaling networks mediate RTK dependent growth and survival in childhood ALL
GSE42054	Diverse phospho-signaling networks mediate RTK dependent growth and survival in childhood ALL [copy number]
GSE42056	Affymetrix SNP array data for acute lymphoblastic leukemia samples
GSE42171	Affymetrix SNP6 array data for ACTH-Independent Macronodular Adrenal Hyperplasia (AIMAH) samples
GSE42271	Elimination of mitochondrial DNA variants by nuclear genome transfer in human oocytes.
GSE42525	Affymetrix SNP array data for follicular lymphoma (FL) and transformed follicular lymphoma (tFL) samples
GSE42624	GeneChip Mapping 500K set and Genome-Wide Human SNP 6.0 Array in meningioma tumors
GSE42631	GeneChip Mapping 500K set and Genome-Wide Human SNP 6.0 Array for glioblastomas
GSE43149	Single-nucleotide polymorphism array analysis reveals distinct chromosomal aberrations in breast cancer tumors according to the circulating tumor cells status
GSE43679	Identification of DNA palindromes in the MCF-7 breast cancer cell line
GSE43934	Whole Genome Characterization of Circulating Tumor Cells Identifies Novel Prognostic Genomic Alterations in Melanoma Metastasis
GSE44019	Affymetrix SNP array data for metastatic melanoma specimens
GSE44549	Genomic changes in low vs high metastatic A549 NSCLC cell line
GSE45000	Genome-wide methylation analysis of prostate tissues reveals global methylation patterns of prostate cancer
GSE45149	The MLH1 c.-27C>A and c.85G>T variants are borne on a European ancestral haplotype which underlies an autosomal dominant form of MLH1 epimutation.
GSE45185	Genetic diversity of propagating/stem cells in glioblastoma multiforme (GBM)
GSE45565	Clonal evolution, genomic drivers, and effects of therapy in chronic lymphocytic leukemia
GSE46594	The self-renewal of gastric cancer stem cells is regulated by a specific collaboration between the microenvironment and the genetic condition.
GSE46598	Integrated epigenomic analyses of enhancer as well as promoter regions in gastric cancer
GSE46745	Genome-wide Genotyping of Acute Myeloid Leukemia with Translocation t(9;11)(p22;q23) Reveals Novel Recurrent Genomic Alterations
GSE46848	The distribution of genomic variations in human iPSCs is related to replication timing reorganization during reprogramming
GSE46951	Clonal evolution in relapsed NPM1 mutated acute myeloid leukemia
GSE46969	Affymetrix SNP array data for 29 MCL cases
GSE47077	Multi-region copy-number analysis
GSE47507	Affymetrix SNP array data for 4 MYC-negative B-cell lymphoma cases and 2 B-cell lymphoma cell lines (SU-DHL-5 and HT)
GSE47508	A recurrent 11q aberration pattern characterizes a subset of MYC-negative mature aggressive B-cell lymphomas resembling Burkitt lymphoma
GSE47646	Generation and Characterization of an immortalized human mesenchymal stromal cell line model [Affymetrix]
GSE47651	Generation and Characterization of an immortalized human mesenchymal stromal cell line model
GSE47914	Genomic instability of human embryonic stem cells in mechanic and enzymatic passaging culture
GSE47917	Genome alterations in human pluripotent stem cells as very early events highly dependent on cell passaging conditions
GSE48064	Respective Prognostic Value of Genomic Grade and Histological Proliferation Markers in Early Stage (pN0) Breast Carcinoma
GSE48190	Affymetrix_SNP6_Allelotyping
GSE48351	Affymetrix SNP6 copy number data on ovarian cancer cell lines
GSE48377	Affymetrix SNP array data for breast cancer samples
GSE49004	Parallel SNP and CGH arrays of cytogenetic normal MDS patients and detection of alterations present in CD3+ T cells and bone marrow cells
GSE49045	Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease)
GSE49215	Genomic characterization of three acute lymphoblastic leukemia cases and one established cell line REH at the single cell level
GSE49396	Affymetrix SNP 6.0 data for analysis of esophageal adenocarcinoma samples
GSE49602	Next-generation sequencing of cancers of unknown primary (Affymetrix GenomeWideSNP data)
GSE49666	Distinct Mutational Patterns of Infection and Non-Infection-Related Bile Duct Cancers Revealed by Exome Sequencing
GSE50024	Affymetrix SNP 6.0 array data for Diffuse Intrinsic Pontine Glioma
GSE50025	Diffuse Intrinsic Pontine Glioma
GSE50252	Genomic profiling of Richter-syndrome Chronic Lymphocytic Leukemia
GSE50253	Genomic profiling of Anaplastic Large Cell Lymphoma
GSE50441	Paternal segmental isodisomy of centromeric region on chromosome 1 as a cause of juvenile hemochromatosis
GSE50667	The pattern of genomic instability during bladder cancer progression (part 2)
GSE50668	The pattern of genomic instability during bladder cancer progression
GSE50973	Analysis of the coding exome of follicular lymphoma
GSE51711	Affymetrix SNP array data for chronic lymphocytic leukemia samples
GSE52788	DNA copy number changes in malignant mesothelioma
GSE53042	Copy number variation comparison between control and CC214-2 resistant GBM39 xenografts
GSE53121	SKOV3 cells comparative genomic hybridization
GSE53436	Affymetrix SNP array data for various human ES cell lines
GSE53790	Mapping of hepatic expression quantitative trait loci (eQTLs) in a Han Chinese population [SNP analysis]
GSE53792	Mapping of Hepatic Expression Quantitative Trait Loci (eQTLs) in a Han Chinese Population
GSE55042	Oncogene-like induction of cellular invasion from centrosome amplification
GSE55153	Epigenome signatures during gastric carcinogenesis based on next generation sequencing [Affymetrix]
GSE55160	Epigenome signatures during gastric carcinogenesis based on next generation sequencing
GSE55395	The distribution of genomic variations in human iPSCs is related to replication timing reorganization during reprogramming [Affymetrix]
GSE55628	Differentially expressed genes and chromosomal alterations in ovarian cancer cell lines sensitive or resistant to a Src-inihibitor, saracatinib
GSE55638	SNP6 profiling of papillary carcinoma of the breast
GSE55640	SNP6 and expression profiling of papillary carcinoma of the breast
GSE56334	Comparative genomic hybridization of CHO Chr6 cell line
GSE57018	Affymetrix SNP array data for adult acute lymphoblastic leukemia samples
GSE57548	SNP6 profiling of metaplastic breast carcinoma
GSE57549	Metaplastic breast carcinomas display genomic and transcriptomic heterogeneity
GSE58232	Genome-wide analysis in Human Colorectal Cells reveals Ischaemia-mediated expression of motility genes via DNA hypomethylation (SNP array)
GSE58233	Genome-wide analysis in Human Colorectal Cells reveals Ischaemia-mediated expression of motility genes via DNA hypomethylation
GSE58579	High-resolution genome-wide copy number analysis of low grade serous ovarian tumours
GSE58951	Single Nucleotide Polymorphisms Other Than Factor V Leiden are Associated with Coagulopathy and Osteonecrosis of the Femoral Head in Chinese Patients
GSE59244	Affymetrix SNP array data for 5q- myelodysplastic syndromes
GSE60168	DNA copy number detection from exome sequencing - Exploiting the off-targets (SNP)
GSE60259	DNA copy number detection from exome sequencing - Exploiting the off-targets
GSE60607	Affymetrix SNP 6.0 data for individuals with Trisomy 21 or Down syndrome
GSE60886	Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups
GSE60899	Genome-wide copy number and allele-specific copy number analysis of choroid plexus tumors (I)
GSE61237	Affymetrix SNP array data for high-grade serous ovarian cancer samples
GSE61323	Integrated Genomic Profiling, Therapy Response And Survival In Adult Acute Myelogenous Leukemia
GSE61578	Gene Expression and HD-SNP6.0 data from Primary Testicular (PTL), Primary Central Nervous System Lymphoma (PCNSL) and Primary Mediastinal B-cell Lymphoma (PMLBCL)
GSE61769	SNP genotyping data from human iPSCs and human fibroblast cells
GSE62215	Affymetrix SNP array data for NF1-associated glioma risk
GSE62407	Affymetrix SNP array data for lung cancer samples
GSE62438	Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
GSE62440	Application of CGH-array and SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
GSE62717	Affymetrix SNP 6.0 array data for ACRG Gastric Cancer Study
GSE62875	Affymetrix SNP array data for colon cancer samples
GSE62907	The inactive X chromosome is epigenetically unstable and transcriptionally labile in breast cancer
GSE62965	Identification of SNPs using genomic DNA and allele specific expression using nascent RNA on snp6 array
GSE63490	Copy number analysis of liver metastases from colorectal cancer
GSE63601	Widespread somatic L1 retrotransposition occurs early during gastrointestinal cancer evolution
GSE63630	The reversed evolution from multicellularity to unicellularity during carcinogenesis
GSE63784	The HDAC inhibitor panobinostat acts as a sensitizer for erlotinib activity in EGFR mutated and wildtype NSCLC cells
GSE64241	Affymetrix SNP copy number data for embryonic stem cell samples
GSE64822	Clinical and molecular characterization of splenic diffuse red pulp lymphomas
GSE65052	Affymetrix SNP-array data for splenic diffuse red pulp lymphoma samples
GSE65424	Combination testing using a single MSH5 variant alongside HLA haplotypes improves coeliac disease risk prediction in the Polish population
GSE65777	A Genome Wide Association Study Reveals Genetic Predisposition for Bortezomib-Induced Peripheral Neuropathy in Multiple Myeloma by Variation in the PREP1-CBS locus.
GSE66070	Mcl-1 is a key determinant of breast cancer cell survival [copy number]
GSE66072	Mcl-1 is a key determinant of breast cancer cell survival
GSE66398	Prospective biomarker analysis of the randomized CHER-LOB study evaluating the dual anti-HER2 treatment with chemotherapy plus trastuzumab and lapatinib as neoadjuvant therapy for HER2-positive breast cancer [copy number]
GSE66399	Prospective biomarker analysis of the randomized CHER-LOB study evaluating the dual anti-HER2 treatment with chemotherapy plus trastuzumab and lapatinib as neoadjuvant therapy for HER2-positive breast cancer
GSE66668	Inherited and somatic defects in DDX41 in myeloid neoplasms
GSE66903	Genome wide association study on neuropathy in multiple myeloma
GSE67047	Genome-wide association and epistatic studies in sporadic medullary and juvenile papillary thyroid carcinomas
GSE67189	Molecular characterization of ovarian serous cystadenomas and fibromas [Copy number]
GSE67224	Molecular characterization of ovarian serous cystadenomas and fibromas
GSE67271	Distinctive genotypes in infants with T-cell acute lymphoblastic leukaemia
GSE67405	Affymetrix SNP array data for B-lineage acute lymphoblastic leukemia
GSE67460	Affymetrix SNP array data for chronic myelomonocytic leukemia samples
GSE67929	Affymetrix SNP Array data for familial coarctation of the aorta (CoA) I
GSE67930	Affymetrix SNP Array data for familial coarctation of the aorta (CoA) II
GSE67965	Patterns of Copy-Number Loss in Gastric Adenocarcinoma
GSE68476	Copy number variation in melanoma biopsy specimens
GSE68717	Genome-wide LOH and DNA copy number alteration in HPV-neg OSCC and their associations with disease-specific survival
GSE68999	Affymetrix SNP array data from BM-CD138+, obtained from newly diagnosed Multiple Myeloma patients
GSE69000	Hedgehog pathway analysis in both CD138+ and B-cells obtained from newly diagnosed Multiple Myeloma patients
GSE69028	Affymetrix SNP array data from BM-CD138+, obtained from newly diagnosed Multiple Myeloma patients [response to VTD therapy]
GSE69029	CD138+ expression and genomic profile obtained from newly diagnosed Multiple Myeloma patients up-front treated with VTD induction therapy
GSE69614	Copy number variation analysis of hepatic metastases from uveal melanoma
GSE70650	Genomic copy number variations in the genomes of leukocytes predict prostate cancer clinical outcomes
GSE70653	Affymetrix Genome-Wide Human SNP Array 6.0 data for Type II Enteropathy-associated T-cell lymphoma
GSE70654	Type II Enteropathy-associated T-cell lymphoma
GSE70770	Prostate cancer stratification using molecular profiles
GSE71443	Affymetrix 6.0 SNP arrays interrogated to detect allele-specific DNA modification in the brain
GSE71522	Affymetrix SNP array data for Ovarian Cancer Samples
GSE71525	A comprehensively characterized cell line panel highly representative of clinical ovarian high-grade serous carcinomas
GSE72660	Integrated Analysis of Genome-Wide DNA Copy Number and Gene Expression with Patient Outcomes in Esophageal Adenocarcinoma [Copy Number]
GSE73076	Prostate cancer stratification using molecular profiles [Stockholm genotype]
GSE73558	Affymetrix SNP6 array data for NLPHL- and PMBCL-derived cell lines
GSE73639	Targeting Non-proteolytic Protein Ubiquitination for the Treatment of Diffuse Large B Cell Lymphoma (Affy SNP6.0 Arrays)
GSE73791	Relapsed diffuse large B-cell lymphoma present different genomic patterns of alterations between early and late relapses
GSE73822	Affymetrix SNP array data for long time/short time survivors
GSE73879	Repression of stress-induced LINE-1 expression protects cancer cell populations from lethal drug-exposures [ChIP-Seq]
GSE74555	Affymetrix SNP array data for HNSCC samples
GSE75284	SNP profiles of 50 HB tumors
GSE75285	mRNA, miRNA and SNP profiles of 50 HB tumors
GSE75312	Affymetrix SNP array data for samples of 9 members of a FNMTC family
GSE75314	A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family A)
GSE75349	A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family B)
GSE75358	A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
GSE76213	Copy Number Variation of human hepatocellular carcinoma (HCC) and Cholangiocarcinoma (CCA) from the Thailand Initiative in Genomics and Expression Research for Liver Cancer (TIGER-LC)
GSE76311	Human hepatocellular carcinoma (HCC) and Cholangiocarcinoma (CCA) from Thailand Initiative in Genomics and Expression Research for Liver Cancer (TIGER-LC)
GSE77557	Affymetrix SNP6.0 array data for EBF1-PDGFRB rearranged acute lymphoblastic leukemia
GSE77775	Affymetrix SNP 6.0 array data for gastric adenocarcinoma and some matched normals
GSE78715	Influence of ATM-mediated DNA damage response on genomic variation in human induced pluripotent stem cells (Affymetrix CNV)
GSE80460	SNP arrays in matched colorectal cancer and normal colonic mucosa.
GSE80526	Genomewide copy number profiles for breast cancer from Taiwanese women
GSE81738	Affymetrix SNP array data for myelodysplastic syndromes samples
GSE83272	Characterisation of the genomic landscape of CRLF2 deregulated acute lymphoblastic leukaemia
GSE83566	Frequent Evolution of Copy Number Alterations Following First‑line Treatment with FC(R) is Enriched with TP53 Alterations which Impact Long Term Survival – Results from the CLL8 Trial
GSE85428	Affymetrix SNP array data for family UNK-129-KW with multiple patients suffering from a lethal form of a primary immunodeficiency.
GSE85466	Epigenomic Profiling of Primary Gastric Adenocarcinoma Reveals Super-enhancer Heterogeneity [SNP]
GSE85467	Epigenomic Profiling of Primary Gastric Adenocarcinoma Reveals Super-enhancer Heterogeneity
GSE85594	A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population
GSE85733	Prospective identification of resistance mechanisms to HSP90 inhibition in KRAS mutant cancer cells [GenomeWideSNP_6]
GSE85734	Prospective identification of resistance mechanisms to HSP90 inhibition in KRAS mutant cancer cells
GSE86621	Expression data from diagnostic samples of diffuse large B-cell lymphomas (DLBCL), follicular lymphoma (FL) and primary and relapsed transformed FL [SNP]
GSE86622	Expression data from diagnostic samples of diffuse large B-cell lymphomas (DLBCL), follicular lymphoma (FL) and primary and relapsed transformed FL
GSE87048	Analysis of somatic DNA copy number alterations and frequency of breast cancer intrinsic subtypes from Mexican women [copy number]
GSE87049	Analysis of somatic DNA copy number alterations and frequency of breast cancer intrinsic subtypes from Mexican women
GSE90073	Genotyping data from Phase 2 of the SAMARA study (Supporting a Multi-disciplinary Approach to Researching Atherosclerosis)
GSE90076	Clinical Evidence Supports a Protective Role for CXCL5 in Coronary Artery Disease Progression in the Elderly
GSE90651	SNP data from hepatocellular carcinoma PDX
GSE90653	Data from hepatocellular carcinoma PDX
GSE91072	Copy number variant (CNV) and Single nucleotide polymorphism (SNP) of UCLA hESC lines
GSE93037	Differentiated Demographic Histories and Local Adaptations between Sherpas and Tibetans
GSE95239	Stratification of clear cell renal cell carcinoma (ccRCC) genomes by gene-directed copy number alteration (CNA) analysis
GSE95496	Affymetrix SNP array data for acute myeloid leukemia samples
GSE95691	SNP array data for acute myeloid leukemia samples
GSE95726	Copy number profiling of prostate cancers from 40 African American patients
GSE96708	Affymetrix SNP6.0 array data for isogenic melanoma cell lines
GSE99002	Resistance to Palbociclib involves multiple mechanisms amenable to targeting with drug holidays or drug switching to improve therapeutic outcome [Affymetrix]
GSE99003	Resistance to Palbociclib involves multiple mechanisms amenable to targeting with drug holidays or drug switching to improve therapeutic outcome
GSE99813	Affymetrix SNP6.0 array data for PAX5 amplified acute lymphoblastic leukemia
GSE100844	SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia
GSE101416	Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity [GenomeWideSNP_6]
GSE101418	Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity
GSE102085	Molecular analysis of high-grade serous ovarian carcinoma with and without associated serous tubal intra-epithelial carcinoma [CNV]
GSE102094	Molecular analysis of high-grade serous ovarian carcinoma with and without associated serous tubal intra-epithelial carcinoma
GSE103342	Characterization of a clival chordoma xenograft model reveals inherent tumor genomic instability
GSE106818	Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
GSE107507	The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses [human SNP array]
GSE107513	The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
GSE107558	Ivy Glioblastoma Atlas Project (SNP)
GSE107560	Ivy Glioblastoma Atlas Project
GSE109360	Integrative genomic analysis in HCC samples [SNP]
GSE109361	Integrative genomic analysis in HCC samples
GSE109813	SNP data of Familial adenomatous polyposis (FAP) organoids
GSE109814	Expression data and SNP data of Familial adenomatous polyposis (FAP) organoids
GSE113496	Genetic defects affecting the development of severe Buruli Ulcer
GSE114183	Medullary breast carcinoma, a triple-negative breast cancer subtype associated with BRCAness.
GSE114269	Medullary breast carcinoma, a triple-negative breast cancer subtype associated with BCLG overexpression and BRCAness
GSE115674	Genomic data from 48 Asian gastric patient-derived xenograft (PDX) models, 7 Asian gastric patient tumors and the 8 corresponding normal tissues
GSE115755	Establishment of patient-derived tumor xenografts from Asian gastric adenocarcinoma is characterized by clonal selection and bias in molecular subtypes
GSE116518	Burkitt-like lymphoma with 11q aberration: A germinal center derived lymphoma without ID3-TCF3-CCND3 pathway deregulation [SNP6]
GSE116527	Burkitt-like lymphoma with 11q aberration: A germinal center derived lymphoma without ID3-TCF3-CCND3 pathway deregulation
GSE118086	Pharmacogenetics and Drug Discovery for Anthracycline-Induced Cardiotoxicity Enabled by Sinoatrial Node-like Cells Derived from Human Pluripotent Stem Cells [SNP array]
GSE118087	Pharmacogenetics and Drug Discovery for Anthracycline-Induced Cardiotoxicity Enabled by Sinoatrial Node-like Cells Derived from Human Pluripotent Stem Cells
GSE119335	RNA over-editing leads to aggressiveness of intrahepatic cholangiocarcinoma [SNP]
GSE119337	RNA over-editing leads to aggressiveness of intrahepatic cholangiocarcinoma
GSE121631	Genome-wide copy number profiling of MCF-7 and fulvestrant-resistant MCF-7/FR cells by SNP microarray.
GSE123011	Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features and clinical outcome
GSE124187	Copy number analysis of BPH (Benign Prostatic Hyperplasia)
GSE125296	SNP array_YW-JTH_NCOMMS-18-17273A
GSE128292	Large B-Cell Lymphomas in Pediatric and Young Adults Display Clinically Relevant Molecular Features Distinguishable from Adult Counterparts [SNP]
GSE128294	Large B-Cell Lymphomas in Pediatric and Young Adults Display Clinically Relevant Molecular Features Distinguishable from Adult Counterparts
GSE128602	Clonal evolution patterns in acute myeloid leukemia with NPM1 mutation (Affymetrix SNP data set)
GSE128604	Clonal evolution patterns in acute myeloid leukemia with NPM1 mutation
GSE128695	An association study between somatic alterations and eQTL in immunity, DNA repair and inflammation pathways in esophageal squamous cell carcinoma (ESCC)
GSE129890	Single nucleotide variants (SNVs) associated with cutaneous melanoma (CM) risk and prognosis
GSE131114	Genomic Alterations in High-risk CLL Frequently Affect Cell Cycle Key Regulators and NOTCH1‑regulated Transcription.
GSE132453	Comorbidities - microcephaly, facial dysmorphia and epilepsy - increase the risk of the pathogenic CNV finding in patients with intellectual disability and autism
GSE135598	TRPS1 drives heterochromatic origin refiring and cancer genome evolution [copy number]
GSE137481	Epithelial Tumour Suppressor ELF3 is a Lineage-Specific Amplified Oncogene in Lung Adenocarcinoma
GSE138438	Copy-number profiling by SNP array of 4 acute myeloid leukemia (AML) cell lines
GSE139294	DNA copy number profiling of lung adenocarcinomas and patient-matched non-malignant lung
GSE144918	Copy number variation analysis in Japanese children with Autsim Spectrum Disorder by Affymetrix Genome-Wide Human SNP Array 6.0.
GSE145846	Key Super Enhancers Drive Tumor-Suppressing Transcription Feedback Programs in Mature B Cell Cancers (SNP array)
GSE145848	Key Super Enhancers Drive Tumor-Suppressing Transcription Feedback Programs in Mature B Cell Cancers
GSE151767	Novel Rare Copy Number Variants Associated with Tetralogy of Fallot in the Han Chinese Population
GSE154591	Genomic comparison of post-radiation versus sporadic sarcomas
GSE156652	The Brazilian Initiative on Precision Medicine (BIPMed)
GSE160982	SNP array of 121 AML patients at diagnosis
GSE178763	Pharmacogenomics characterization of the MDM2 inhibitor MI-773 reveals candidate tumours and predictive biomarkers
GSE196183	Affymetrix SNP Data array data of pancreatic cancer PDX models
GSE207762	Integrative Genomic Analysis of Medulloblastoma Identiﬁes a Molecular Subgroup That Drives Poor Clinical Outcome [DNA copy number]
GSE267025	SNP arrays in colorectal adenocarcinoma cell lines

Data table
ID	Chromosome	RANGE_GB	RANGE_START	RANGE_STOP	STRAND	Physical Position	SNP_ID	Allele A	Allele B
SNP_A-1780419	1	NC_000001.10			-	84875173	rs6576700	A	G
SNP_A-1780418	5	NC_000005.9			-	156390980	rs17054099	C	T
SNP_A-1780415	5	NC_000005.9			-	158729947	rs7730126	A	G
SNP_A-1780414	9	NC_000009.11			+	22976592	rs2061700	A	C
SNP_A-1780413	11	NC_000011.9			+	26300969	rs10834942	A	G
SNP_A-1780412	5	NC_000005.9			+	123078585	rs17419765	C	T
SNP_A-1780379	13	NC_000013.10			+	77436808	rs7995987	G	T
SNP_A-1780410	2	NC_000002.11			+	225226512	rs16865866	A	G
SNP_A-1780378	8	NC_000008.10			-	119412451	rs7828844	A	G
SNP_A-1780377	11	NC_000011.9			+	6409790	rs11040883	A	G
SNP_A-1780376	6	NC_000006.11			-	169952778	rs730002	A	G
SNP_A-1780375	7	NC_000007.13			-	12987060	rs2024406	A	G
SNP_A-1780374	2	NC_000002.11			-	135285678	rs515983	A	G
SNP_A-1780373	14	NC_000014.8			+	75267941	rs2287407	A	G
SNP_A-1780372	6	NC_000006.11			+	3622751	rs35877559	C	T
SNP_A-1780371	9	NC_000009.11			-	119583730	rs10759862	A	G
SNP_A-1780370	2	NC_000002.11			+	227268591	rs13032261	A	C
SNP_A-1780409	4	NC_000004.11			-	159982551	rs34227797	C	G
SNP_A-1780408	14	NC_000014.8			+	27493392	rs1245317	G	T
SNP_A-1780405	15	NC_000015.9			-	58479008	rs17240650	A	G