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GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000240308

Variant: GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3

Type: Variant
Allele: GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3 247968
Gene:
Type: copy number gain
Location: Chr11: 115215434 - 120559928 - assembly GRCh37

Condition

PhenotypeInstruction: See cases