GEO DataSets

(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

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(Submitter supplied) Agilent Custom Human 244K CGH Microarray consisting of 60-mer oligonucleotides mapped to human genome build 35. Reference: de Smith et al, Human Molecular Genetics, 2007 Protocol: see manufacturer's web site at http://www.agilent.com/

Organism:

Homo sapiens

1 Series

57 Samples

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