Deletion (Genetics)
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High Quality Content by WIKIPEDIA articles! In genetics, a deletion is a mutation in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of genetic material. Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome. Deletions can be caused by errors in chromosomal crossover during meiosis. This causes several serious genetic diseases. Causes include the following: losses from translocation, chromosomal, crossovers within a chromosomal inversion, unequal crossing over, breaking without rejoining. For synapsis to occur between a...
High Quality Content by WIKIPEDIA articles! In genetics, a deletion is a mutation in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of genetic material. Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome. Deletions can be caused by errors in chromosomal crossover during meiosis. This causes several serious genetic diseases. Causes include the following: losses from translocation, chromosomal, crossovers within a chromosomal inversion, unequal crossing over, breaking without rejoining. For synapsis to occur between a chromosome with a large intercalary deficiency and a normal complete homolog, the unpaired region of the normal homolog must loop out of the linear structure into a deletion or compensation loop.
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