ISCA-37392-Loss

7q11.23 recurrent (Williams-Beuren syndrome) region (includes ELN) Loss
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
194050, Williams syndrome