GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.2(chr11:14498547-14855923)x3 AND not provided

Significance: Benign
ClinVar: RCV000749958

Variant: GRCh37/hg19 11p15.2(chr11:14498547-14855923)x3

Type: Variant
Allele: GRCh37/hg19 11p15.2(chr11:14498547-14855923)x3 604658
Gene:
Type: copy number gain
Location: Chr11: 14498547 - 14855923 - assembly GRCh37

Condition

Disease: not provided