[svtoolkit-help] Inquiry about Genome STRiP

[Young-jun K. <you...@gm...>]

Dear, webmaster

I'm a graduate student in SNU, Seoul, Korea.

I used Genome STRiP for detecting CNVs, and Output vcf files were gained.

Among the results, I found that there were some overlapped CNV regions or
some regions include other regions.

Despite I considered combination of allele types, results were illogical.

(real ex - all of 26 individuals have hetero(0/1) types,
93755407-93818770, 93755562-93818886, 93756831-93821153,
93757996-93821773,.........)


How do I have to handle this kind of result?


Thank you.

sincerely, Young-jun