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GRCh38/hg38 11p15.4(chr11:7187414-7707594)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000139155

Variant: GRCh38/hg38 11p15.4(chr11:7187414-7707594)x3

Type: Variant
Allele: GRCh38/hg38 11p15.4(chr11:7187414-7707594)x3 160023
Gene:
Type: copy number gain
Location: Chr11: 7208645 - 7729141 - assembly GRCh37
Chr11: 7165221 - 7685717 - assembly NCBI36
Chr11: 7187414 - 7707594 - assembly GRCh38
Chr11: 7187414 - 7707594 - assembly GRCh38
References: dbVar: nsv916533
dbVar: nssv1603436

Condition

PhenotypeInstruction: See cases