Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

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Table 1.

CNV coverage by chromosome

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Table 1.

Sample-level CNVs refer to CNVs detected in individual DNA samples, and CNV events refer to all independent CNVs. CNV events are merged for regions sharing at least 30% of SNPs. Gain, Loss, and Gain + loss refer to CNVs that are found only as insertions, only as deletions, or as both insertions and deletions, respectively, in the HapMap set.

This Article

  1. Genome Res. 16: 1575-1584

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