GSM1722[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 2000000491.

DNA copy-number changes

(Submitter supplied) Gene amplifications and deletions frequently contribute to tumorigenesis. Characterization of these DNA copy-number changes is important for both the basic understanding of cancer and its diagnosis. Comparative genomic hybridization (CGH) was developed to survey DNA copy-number variations across a whole genome. With CGH, differentially labelled test and reference genomic DNAs are co-hybridized to normal metaphase chromosomes, and fluorescence ratios along the length of chromosomes provide a cytogenetic representation of DNA copy-number variation. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by array

Platform:: GPL179
10 Samples

Download data

Series

Accession:: GSE49

ID:: 200000049

Select item 1000001792.

SVA

(Submitter supplied) A microarray with 6720 spot features. Tip Configuration: Standard 4-tip Columns per Sector: 42 Rows per Sector: 40 Column Spacing: 157 Row Spacing: 157