Test what evidence supports the presence of a CNV in an ExomeDepth object.
TestCNV(x, chromosome, start, end, type)
ExomeDepth object containing the likelihood information.
Chromosome data (factor
)
Start of the putative CNV
End of the putative CNV
character
, Should be either 'deletion' or 'duplication'
A Bayes factor assessing the evidence in favoor of the CNV.