GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh38/hg38 11p15.4(chr11:7691246-7796490)x1 AND See cases

Significance: Benign
ClinVar: RCV000136762

Variant: GRCh38/hg38 11p15.4(chr11:7691246-7796490)x1

Type: Variant
Allele: GRCh38/hg38 11p15.4(chr11:7691246-7796490)x1 157347
Gene:
Type: copy number loss
Location: Chr11: 7712477 - 7818037 - assembly GRCh37
Chr11: 7669053 - 7774613 - assembly NCBI36
Chr11: 7691246 - 7796490 - assembly GRCh38
Chr11: 7691246 - 7796490 - assembly GRCh38
References: dbVar: nsv534106
dbVar: nssv581561

Condition

PhenotypeInstruction: See cases