GENETIC ENCYCLOPEDIA
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GRCh37/hg19 11p15.3(chr11:11970971-11986061)x3 AND not provided

Significance: Benign
ClinVar: RCV000737431

Variant: GRCh37/hg19 11p15.3(chr11:11970971-11986061)x3

Type: Variant
Allele: GRCh37/hg19 11p15.3(chr11:11970971-11986061)x3 592131
Gene:
Type: copy number gain
Location: Chr11: 11970971 - 11986061 - assembly GRCh37

Condition

Disease: not provided