ISCA-37486-Loss

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green ISCA-37486-Loss Region in Common deletion and duplication syndromes


Version 0.137

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Chromosome 16p11.2 deletion syndrome, MIM#611913, distal BP2-BP3
  • intellectual disability
  • autism
  • obesity
Tags
  • SV/CNV