GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 15q11.2-13.1(chr15:22770421-28828168)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000446646

Variant: GRCh37/hg19 15q11.2-13.1(chr15:22770421-28828168)x1

Type: Variant
Allele: GRCh37/hg19 15q11.2-13.1(chr15:22770421-28828168)x1 384250
Gene:
Type: copy number loss
Location: Chr15: 22770421 - 28828168 - assembly GRCh37
References: dbVar: nsv2778726
dbVar: nssv13650536

Condition

PhenotypeInstruction: See cases