Hi, I have used XHMM to identify CNVs from our exomes. But for many cases the high score deletions/duplication called by XHMM are not getting correlated with visualization of bam through IGV. If a region is called as deletion in only one individual by XHMM and when we visualize the region through IGV, the region has same coverage when compared to other exomes. Can anyone explain me why this is happening and how can i rectify this?
As you said it may be because I am using the bam which is not normalized for library size. Still we could get some hint from bam (am I right?). Xhmm result is as follow 2180 DEL X:13762483-13786394 23.91 X 13774438 201446..201462 17 32 99 99 33 11 -2.68 47.8