GSM496231[Accession] - GEO DataSets

Warning: The NCBI web site requires JavaScript to function. more...

Format

Summary
Summary (text)
Unique Identifier List

Sort by

Default order
Number of Samples (High to Low)
Number of Samples (Low to High)

Send to:

Choose Destination

File
Clipboard
Collections

Search results

Items: 3

Select item 2000196511.

Discovery of common Asian copy number variants using high-resolution array CGH

(Submitter supplied) Discovery of common Asian copy number variants using a novel integrated high-resolution array CGH and massively parallel DNA sequencing. We attempted to discover common Asian copy number variants (CNVs) from the DNA of 30 Asian women (10 Korean, 10 CHB (HapMap), 10 JPT (HapMap)) using a custom-designed 24M-oligonucleotide Agilent platform (1.1M X 24 slides). The reference sample for aCGH was NA10851 (HapMap CEPH). more...

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

24 related Platforms
792 Samples

Download data: TXT

Series

Accession:: GSE19651

ID:: 200019651

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000098842.

Agilent/SNU human 24M CGH array, 13 of 24 (Feature Number version)

(Submitter supplied) Custom-designed 24M-oligonucleotide whole-genome array (1.1M X 24 slides). Probes correspond to human genome build UCSC hg18 (NCBI Build 36). Protocol: See manufacturer's web site (www.Agilent.com).