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GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000136773

Variant: GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1

Type: Variant
Allele: GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1 157358
Gene:
Type: copy number loss
Location: Chr11: 10011063 - 16847353 - assembly GRCh37
Chr11: 9967639 - 16803929 - assembly NCBI36
Chr11: 9989516 - 16825806 - assembly GRCh38
Chr11: 9989516 - 16825806 - assembly GRCh38
References: dbVar: nsv534118
dbVar: nssv582152

Condition

PhenotypeInstruction: See cases