GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.1(chr11:16820813-18103432)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000449180

Variant: GRCh37/hg19 11p15.1(chr11:16820813-18103432)x3

Type: Variant
Allele: GRCh37/hg19 11p15.1(chr11:16820813-18103432)x3 384057
Gene:
Type: copy number gain
Location: Chr11: 16820813 - 18103432 - assembly GRCh37
References: dbVar: nsv2777419
dbVar: nssv13652917

Condition

PhenotypeInstruction: See cases