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Fig. 3 | BMC Bioinformatics

Fig. 3

From: PennCNV in whole-genome sequencing data

Fig. 3

PennCNV plot of Log R Ratio (coverage) and B Allele Frequency for a zero-copy (CN=0) deletion in simulated data. It is possible to see how the coverage is much lower than the average and the lack of data for allele frequency, as there are just very few reads mapped in the read

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