GSM248019[Accession] - GEO DataSets

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Items: 3

Select item 2000098311.

The fine-scale and complex architecture of human copy number variation

(Submitter supplied) Despite considerable excitement over the potential functional significance of copy number variants (CNVs), we still lack knowledge of the fine-scale architecture of the large majority of CNV regions in the human genome. In this study, we used a high-resolution array-based comparative genomic hybridization (aCGH) platform that targeted known CNV regions of the human genome at ~1 kb resolution to interrogate the genomic DNAs of 30 individuals from four HapMap populations. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

Platforms:: GPL6251 GPL6250
144 Samples

Download data: TXT

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Accession:: GSE9831

ID:: 200009831

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000062502.

Agilent-015685 Custom Human 244K CGH Microarray

(Submitter supplied) Agilent Custom Human 244K CGH Microarray consisting of 60-mer oligonucleotides publication: Perry et al. Nature Genetics, 2007 Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The FeatureNum column represents the Agilent Feature Extraction feature number. more...