25 January 2019 1 4K Report

I am confused about the copy number variation. I only have SNPs data from illumina SNPs arrays. I can use many tools to detection the CNV.

But I want to know is

for example, a family CNV analysis:

A child has deletion from father. how do I find out the location of this deletion in father's chromosome? And is it in the forward strand or reverse strand?

Many thanks

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