GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.2(chr11:14513629-14816556)x3 AND not provided

Significance: Uncertain significance
ClinVar: RCV000849855

Variant: GRCh37/hg19 11p15.2(chr11:14513629-14816556)x3

Type: Variant
Allele: GRCh37/hg19 11p15.2(chr11:14513629-14816556)x3 676756
Gene:
Type: copy number gain
Location: Chr11: 14513629 - 14816556 - assembly GRCh37

Condition

Disease: not provided