GSM1341035[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 2000556451.

Genome wide analysis of copy number variation in NAFLD spectrum

(Submitter supplied) Despite some success in identifying CNVs responsible for metabolic phenotypes including obesity and diabetes mellitus, there are as yet no data available to suggest whether or not CNVs might be involved in the etiology of the NAFLD spectrum. This report is a comprehensive analysis of copy number in Malaysian patients with NAFLD.

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

Platform:: GPL9777
49 Samples

Download data: TXT

Series

Accession:: GSE55645

ID:: 200055645

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000097772.

Agilent-021850 SurePrint G3 Human CGH Microarray (Feature Number version)

(Submitter supplied) SurePrint G3 Human CGH Microarray 2x400K Arrays of this design have barcodes that begin with 16021850 or 2521850. 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 ID column represents the Agilent Feature Extraction feature number. more...