I would like to call CNVs with GermlineCNVCaller, but I don't have a large cohort. I do have access to multiple trios, but they are generated over many years, so the sequencing and library preps are quite different. Is it reasonable to make a model using public data instead, like 1000 Genomes? If so, I'd maybe expect that someone had done it already and I could download it, but I can't find anything like that.
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