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GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3 AND not provided

Significance: Pathogenic
ClinVar: RCV000848151

Variant: GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3

Type: Variant
Allele: GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3 675044
Gene:
Type: copy number gain
Location: Chr11: 117830263 - 134938470 - assembly GRCh37

Condition

Disease: not provided