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GRCh37/hg19 11p15.2(chr11:14460052-15556068)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000510874

Variant: GRCh37/hg19 11p15.2(chr11:14460052-15556068)x3

Type: Variant
Allele: GRCh37/hg19 11p15.2(chr11:14460052-15556068)x3 436069
Gene:
Type: copy number gain
Location: Chr11: 14460052 - 15556068 - assembly GRCh37
References: dbVar: nsv2772989
dbVar: nssv13639261

Condition

PhenotypeInstruction: See cases