GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.1(chr11:16436272-18064677)x3 AND not provided

Significance: Uncertain significance
ClinVar: RCV000848487

Variant: GRCh37/hg19 11p15.1(chr11:16436272-18064677)x3

Type: Variant
Allele: GRCh37/hg19 11p15.1(chr11:16436272-18064677)x3 675388
Gene:
Type: copy number gain
Location: Chr11: 16436272 - 18064677 - assembly GRCh37

Condition

Disease: not provided