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Table 3 Summary of CNV regions on chromosome 22 using HMM algorithm for 1,266 subjects that passed PennCNV and CRLMM QC metrics

From: Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform

Software

Number CNVs

Duplications

Deletions

Median Number CNVs per patient (Min, 25%, 75%, Max)

CRLMM/VanillaIce

45,757

7,958

37,799

30 (4, 21, 42, 438)

PennCNV

50,908

16,132

34,776

39 (13, 31, 48, 96)