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GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000512477

Variant: GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3

Type: Variant
Allele: GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 435647
Gene:
Type: copy number gain
Location: Chr11: 230615 - 31995219 - assembly GRCh37
References: dbVar: nsv2770627
dbVar: nssv13652868

Condition

PhenotypeInstruction: See cases