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Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males

(Submitter supplied) The discovery of copy number variation in healthy individuals is far from complete, and due to the resolution of detection systems used, the majority of loci reported so far are relatively large (~65% > 10kb). Applying a two-stage high-resolution array CGH approach to analyse 50 healthy Caucasian males from northern France, we discovered 2208 copy number variants (CNVs) detected by more than one consecutive probe. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL5693
57 Samples
Download data: TXT
Series
Accession:
GSE8691
ID:
200008691

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