C166408Level 6
Chromosome Arm 19q Loss of Heterozygosity
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular abnormality that results in monoallelic loss of function mutations located within the long arm of chromosome 19 (19q).
**Synonyms:** - 19q LOH - 19q Loss of Heterozygosity - Chromosome 19q Loss of Heterozygosity
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