GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.1(chr11:17899742-18258290)x3 AND not specified

Significance: Likely benign
ClinVar: RCV000487464

Variant: GRCh37/hg19 11p15.1(chr11:17899742-18258290)x3

Type: Variant
Allele: GRCh37/hg19 11p15.1(chr11:17899742-18258290)x3 411541
Gene:
Type: copy number gain
Location: Chr11: 17885151 - 18266836 - assembly GRCh37

Condition

Disease: not specified