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This session is intended to give a “typical” end-to-end case review process for CNV/AOH/Seq Var data. At least one example should show a combination of array and NGS. It should follow similar flow as the cyto but should include cases where there is only pathogenic Seq var data as well as potential combination of Seq Var and CNV/AOH (I think the p53 case from CHLA would be very nice here as the last example).