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

Click on image to view larger version.

Table 2.

The CNV calling results for 112 HapMap individuals

Click on table to view larger version.

Table 2.

After using family information, more CNVs with smaller sizes are detected in the CEU and YRI populations.

This Article

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

Preprint Server



Current Issue

  1. March 2026, 36 (3)
  1. Current Issue
  1. Alert me to new issues of Genome Research