PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

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Table 4.

Immunoglobulin-related genomic regions that show elevated frequencies of CNVs in cell line samples (HapMap cohort and AGRE cohort) compared to whole-blood samples

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Table 4.

The increased prevalence of CNVs surrounding IGKC is less obvious, mainly because of low coverage of SNP markers in this region.

This Article

  1. Published in Advance October 5, 2007, doi: 10.1101/gr.6861907 Genome Res. 17: 1665-1674

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