Copy number variation and mosaicism

Amanda Notini, Jeffrey Craig, Stefan White

Research output: Contribution to journalArticleResearchpeer-review

40 Citations (Scopus)

Abstract

Mosaicism is the presence of cells within an organism that have a different genetic composition despite deriving from a single zygote. The consequence of this depends on the number and type of cells that are affected as well as the specific DNA involved. There are several diseases where mosaicism is known to occur, but the currently observed frequency is presumably an underestimation due to the difficulty of detecting changes in only a percentage of cells. Recent advances in technology have provided a greater insight into the frequency and mechanisms of mosaicism in all forms. This review will cover the different techniques that can be used for detecting copy number variation (CNV) in mosaic form, and describe some of the insights that different diseases have given on the true frequencies and mechanisms responsible for somatic rearrangements. It will conclude with a discussion of the implications of the recent description of CNV in identical twins, and what remains to be elucidated in the world of mosaic CNV.
Original languageEnglish
Pages (from-to)270 - 277
Number of pages8
JournalCytogenetic and Genome Research
Volume123
Issue number1-4
DOIs
Publication statusPublished - 2008
Externally publishedYes

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