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 1.

Hidden states, copy numbers, and their descriptions

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Table 1.

Each state has a different distribution of CNV genotypes.

This Article

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

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