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GRCh37/hg19 11p15.2(chr11:14504463-14909461)x1 AND Thyroid hemiagenesis

Significance: Likely pathogenic
ClinVar: RCV000488887

Variant: GRCh37/hg19 11p15.2(chr11:14504463-14909461)x1

Type: Variant
Allele: GRCh37/hg19 11p15.2(chr11:14504463-14909461)x1 354199
Gene:
Type: copy number loss
Location: Chr11: 14504463 - 14909461 - assembly GRCh37

Condition

Finding: Thyroid hemiagenesis