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GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000512225

Variant: GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3

Type: Variant
Allele: GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 435449
Gene:
Type: copy number gain
Location: Chr11: 230615 - 25584362 - assembly GRCh37
References: dbVar: nsv2769639
dbVar: nssv13641100

Condition

PhenotypeInstruction: See cases