GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.2(chr11:14508698-14865666)x3 AND not provided

Significance: Benign
ClinVar: RCV000749959

Variant: GRCh37/hg19 11p15.2(chr11:14508698-14865666)x3

Type: Variant
Allele: GRCh37/hg19 11p15.2(chr11:14508698-14865666)x3 604659
Gene:
Type: copy number gain
Location: Chr11: 14508698 - 14865666 - assembly GRCh37

Condition

Disease: not provided