Andere Kunden interessierten sich auch für
![Genetic of Copy Number Variation]( "Genetic of Copy Number Variation")
Genetic of Copy Number Variation32,99 €![GENETIC BASIS OF VARIATION FOR EARLINESS]( "GENETIC BASIS OF VARIATION FOR EARLINESS")
GENETIC BASIS OF VARIATION FOR EARLINESS38,99 €![Genomic Profile of the Rongmei (Kabui) tribe of Manipur, India]( "Genomic Profile of the Rongmei (Kabui) tribe of Manipur, India")
Genomic Profile of the Rongmei (Kabui) tribe of Manipur, India32,99 €![Somaclonal Variation in some species of Brassica]( "Somaclonal Variation in some species of Brassica")
Somaclonal Variation in some species of Brassica32,99 €![Genetic Variation of Juniperus procera Hochst. ex Endl.]( "Genetic Variation of Juniperus procera Hochst. ex Endl.")
Genetic Variation of Juniperus procera Hochst. ex Endl.32,99 €![The Variation and Adaptive Expression of Antibodies]( "The Variation and Adaptive Expression of Antibodies")
The Variation and Adaptive Expression of Antibodies60,00 €![Theories of Population Variation in Genes and Genomes]( "Theories of Population Variation in Genes and Genomes")
Theories of Population Variation in Genes and Genomes138,99 €
A copy number variation (CNV ) is a segment of DNA in which copy-number differences have been found by comparison of two or more genomes. The segment may range from one kilobase to several megabases in size.Humans (being diploid) ordinarily have two copies of each autosomal region, one per chromosome. This may vary for particular genetic regions due to deletion or duplication.CNVs may either be inherited or caused by de novo mutation. A recently proposed mechanism for the cause of some CNVs is fork stalling and template switching, a replication misstep.