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GRCh37/hg19 11q13.4(chr11:73444963-73777547)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447257

Variant: GRCh37/hg19 11q13.4(chr11:73444963-73777547)x3

Type: Variant
Allele: GRCh37/hg19 11q13.4(chr11:73444963-73777547)x3 383463
Gene:
Type: copy number gain
Location: Chr11: 73444963 - 73777547 - assembly GRCh37
References: dbVar: nsv2773592
dbVar: nssv13655354

Condition

PhenotypeInstruction: See cases