GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.1(chr11:17142196-18014467)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000511047

Variant: GRCh37/hg19 11p15.1(chr11:17142196-18014467)x3

Type: Variant
Allele: GRCh37/hg19 11p15.1(chr11:17142196-18014467)x3 437191
Gene:
Type: copy number gain
Location: Chr11: 17142196 - 18014467 - assembly GRCh37
References: dbVar: nsv3109671
dbVar: nssv14082326

Condition

PhenotypeInstruction: See cases