GENETIC ENCYCLOPEDIA
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GRCh37/hg19 16p11.2(chr16:29595483-29733872)x1 AND not provided

Significance: Benign
ClinVar: RCV000739118

Variant: GRCh37/hg19 16p11.2(chr16:29595483-29733872)x1

Type: Variant
Allele: GRCh37/hg19 16p11.2(chr16:29595483-29733872)x1 593818
Gene:
Type: copy number loss
Location: Chr16: 29595483 - 29733872 - assembly GRCh37

Condition

Disease: not provided