validation approach for CNVs

Question

[heureuse]

Hello,

I'm building a pipeline to call CNV using WGS data. I need to validate my CNV (sensitivity, specifity, etc). I have the genome from GIAB for a first validation. My question is do you know other approaches to validate my CNVs ?

Thanks

[WouterDeCoster]

If you are working with short-read sequencing data, a good solution would be to compare those calls with those from the same sample sequenced with long reads.

[Pierre Lindenbaum]

how is it different from your previous question ? Mendelian precison

[heureuse]

Mendelian Precision is an approach i wanted to use but i'm no longer using it.