GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11q13.3(chr11:69582976-69660482)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000446615

Variant: GRCh37/hg19 11q13.3(chr11:69582976-69660482)x1

Type: Variant
Allele: GRCh37/hg19 11q13.3(chr11:69582976-69660482)x1 384178
Gene:
Type: copy number loss
Location: Chr11: 69582976 - 69660482 - assembly GRCh37
References: dbVar: nsv2778261
dbVar: nssv13648186

Condition

PhenotypeInstruction: See cases