C219070Level 7
11p15 Loss of Heterozygosity
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular abnormality characterized by monoallelic loss of function mutations within the p15 band on the short arm of chromosome 11.
**Synonyms:** - 11p15 LOH - Chromosome 11p15 Loss of Heterozygosity - Chromosome Band 11p15 Loss of Heterozygosity - LOH 11p15 - LOH of Chromosome 11p15
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