What does LOH mean in Human Genome?
This page is about the meanings of the acronym/abbreviation/shorthand LOH in the Medical field in general and in the Human Genome terminology in particular.
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What does LOH mean?
- Loss of heterozygosity
- Loss of heterozygosity. Most diploid cells, for example human somatic cells, contain two copies of the genome, one from each parent; each copy contains approximately 3 billion bases. For the majority of positions in the genome the base present is consistent between individuals, however a small percentage may contain different bases and these positions are called ‘single nucleotide polymorphisms’ or ‘SNPs’. When the genomic copies derived from each parent have different bases for these polymorphic regions the region is said to be heterozygous. The majority of the genome within somatic cells of individuals are heterozygous. However, one parental copy of a region can sometimes be lost, resulting in the region lacking differences at these polymorphic loci and therefore showing loss of heterozygosity. Loss of heterozygosity due to loss of one parental copy in a region is also called hemizygosity in that region.