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GRCh37/hg19 11p14.3(chr11:22225348-22247541)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447189

Variant: GRCh37/hg19 11p14.3(chr11:22225348-22247541)x3

Type: Variant
Allele: GRCh37/hg19 11p14.3(chr11:22225348-22247541)x3 381594
Gene:
Type: copy number gain
Location: Chr11: 22225348 - 22247541 - assembly GRCh37
References: dbVar: nsv2773843
dbVar: nssv13645733

Condition

PhenotypeInstruction: See cases