explain Translocation.

Answer 1

Translocation is a type of genetic mutation in which a chromosome or a segment of a chromosome is moved from one position to another. This can occur between two non-homologous chromosomes, or between two parts of the same chromosome. Translocation can cause a variety of genetic disorders, including Down syndrome, Klinefelter syndrome, and Turner syndrome. It can also cause infertility, miscarriages, and birth defects.