Ataxia and cerebellar anomalies - narrow panel
Region: ISCA-37404-Loss15q11q13 recurrent (PWS/AS) region (BP1-BP3, Class 1) Loss
The required percent of overlap for this region has been changed from 80% to 60% and the genomic location has been updated inline with ClinGen following NHS Genomic Medicine Service approval.Created: 16 Mar 2022, 12:54 p.m. | Last Modified: 16 Mar 2022, 12:54 p.m.
Panel Version: 2.289
GRCh38 position for ISCA-37404-Loss was changed from 22782170-28134729 to 22782170-28134728. Required Overlap Percentage for ISCA-37404-Loss was changed from 80 to 60.
Checked against super panel made up of the panel constituents. Ready to promote to version 1.
Region: ISCA-37404-Loss was added Region: ISCA-37404-Loss was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for Region: ISCA-37404-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for Region: ISCA-37404-Loss were set to 7611294; 22045295 Phenotypes for Region: ISCA-37404-Loss were set to microcephaly; Developmental delay, muscle weakness; 176270; 105831; Angelman syndrome; Prader-Willi syndrome; Mental retardation