Dataset features

Specifications


Application: aCGH data analysis
Number of samples: 12
Release date: Feb 17 2008
Last update date: Mar 19 2012
Access: Public
Diseases: Prader-Willi Syndrome
Genes: BP4, BP5, CHRNA7, BP3
Dataset link Recurrent 15q13 microdeletions

Experimental Protocol


Patients were intially screened by BAC array CGH (n=290) or qPCR (n=1040). Patients with potential 15q13 deletions were then analyzed on a custom oligonucleotide array targeted to the 15q13 region, results of which are shown here.

Repositories


GEO

GSE10189

ArrayExpress

E-GEOD-10189

BioProject

PRJNA108297

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Contact


Heather Mefford