Copy number variation is such a phenomenon in which the number of copies of genes varies from individual to individual. It is a kind of structural variation in which a stretch of DNA might be duplicated, triplicated or quadruplicated. When the Human Genome Project was completed, it was revealed that the genome goes through certain gains as well as losses of genetic material.
This has not been resolved yet that to what extent the copy number variation contributes to the development of the diseases in humans. But it has been known that there are certain types of cancer which are associated when there is an increase in the copy numbers of particular genes.
Meiotic nondisjunction is much more likely than mitotic nondisjunction. Based on
A woman who is heterozygous, Bb, has brown eyes;
Explain why familial breast cancer shows a dominant pattern of inheritance in
How is an F′ factor different from an F factor?
With regard to the timing of conjugation, explain why the recipient
The raw material for evolution is random mutation. Discuss whether or
Why is an antibody used in this experiment? From
Explain the type of speciation (allopatric, parapatric, or sympatric
In fruit flies, curved wings are recessive to straight wings,
A recessive allele in mice results in an unusally long neck.
