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GRCh38/hg38 11p15.4(chr11:7665298-7796490)x1 AND See cases

Significance: Benign
ClinVar: RCV000136767

Variant: GRCh38/hg38 11p15.4(chr11:7665298-7796490)x1

Type: Variant
Allele: GRCh38/hg38 11p15.4(chr11:7665298-7796490)x1 157352
Gene:
Type: copy number loss
Location: Chr11: 7686529 - 7818037 - assembly GRCh37
Chr11: 7643105 - 7774613 - assembly NCBI36
Chr11: 7665298 - 7796490 - assembly GRCh38
Chr11: 7665298 - 7796490 - assembly GRCh38
References: dbVar: nsv534111
dbVar: nssv581569

Condition

PhenotypeInstruction: See cases