In genetics, a centimorgan (abbreviated cM) or map unit (m.u.) is a unit of recombinant frequency for measuring genetic linkage. It is often used to imply distance along a chromosome. The number of base-pairs it corresponds to varies widely across the genome (different regions of a chromosome have different propensities towards crossover), and is about 1 million base pairs in humans[1] [2]. The centimorgan is equal to a 1% chance that a marker at one genetic locus on a chromosome will be separated from a marker at a second locus due to crossing over in a single generation. A 50 cM distance means that the genes will reassort when an odd number of crossings happen, which happens 31.8% of the time. Note that non-syntenic genes are inherently unlinked, and cM distances have no meaning between them. The centimorgan was named in honor of geneticist Thomas Hunt Morgan by his student Alfred Henry Sturtevant. Note that the parent unit of the centimorgan, the morgan, is rarely used today.
References
- ^ http://rarediseases.info.nih.gov/asp/resources/glossary_a-e.asp#C
- ^ Matthew P Scott, Paul Matsudaira, Harvey Lodish, James Darnell, Lawrence Zipursky, Chris A Kaiser, Arnold Berk, Monty Krieger (2004). Molecular Cell Biology, Fifth Edition. San Francisco: W. H. Freeman, 396. ISBN 0-7167-4366-3. “"...in humans 1 centimorgan on average represents a distance of about 7.5x10E5 base pairs"”
