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- Copy-number_variation abstract "Copy-number variations (CNVs)—a form of structural variation—are alterations of the DNA of a genome that results in the cell having an abnormal or, for certain genes, a normal variation in the number of copies of one or more sections of the DNA. CNVs correspond to relatively large regions of the genome that have been deleted (fewer than the normal number) or duplicated (more than the normal number) on certain chromosomes. For example, the chromosome that normally has sections in order as A-B-C-D might instead have sections A-B-C-C-D (a duplication of "C") or A-B-D (a deletion of "C").This variation accounts for roughly 12% of human genomic DNA and each variation may range from about one kilobase (1,000 nucleotide bases) to several megabases in size. CNVs contrast with single-nucleotide polymorphisms (SNPs), which affect only one single nucleotide base.".
- Copy-number_variation thumbnail Gene-duplication.png?width=300.
- Copy-number_variation wikiPageExternalLink CNVannotator.
- Copy-number_variation wikiPageExternalLink cnv.chop.edu.
- Copy-number_variation wikiPageExternalLink pdb.top46.
- Copy-number_variation wikiPageExternalLink 061122-human-genetics.html.
- Copy-number_variation wikiPageExternalLink variation.
- Copy-number_variation wikiPageExternalLink new-research-sheds-light-on-autism%E2%80%99s-genetic-causes.
- Copy-number_variation wikiPageExternalLink www.1000genomes.org.
- Copy-number_variation wikiPageExternalLink www.biodiscovery.com.
- Copy-number_variation wikiPageExternalLink cnfarms.html.
- Copy-number_variation wikiPageExternalLink cnmops.html.
- Copy-number_variation wikiPageExternalLink 4371084a.html.
- Copy-number_variation wikiPageExternalLink nbt.1600.pdf.
- Copy-number_variation wikiPageExternalLink ng0904-931.html.
- Copy-number_variation wikiPageExternalLink ng0707s-S1.pdf.
- Copy-number_variation wikiPageExternalLink query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstract&list_uids=10471496.
- Copy-number_variation wikiPageExternalLink article.ns?id=mg18324592.000.
- Copy-number_variation wikiPageExternalLink dn10646-gene-duplications-may-define-who-you-are-.html.
- Copy-number_variation wikiPageExternalLink cnv.
- Copy-number_variation wikiPageExternalLink copy-number-variation.html.
- Copy-number_variation wikiPageExternalLink cnv.
- Copy-number_variation wikiPageID "3248511".
- Copy-number_variation wikiPageRevisionID "606334239".
- Copy-number_variation hasPhotoCollection Copy-number_variation.
- Copy-number_variation subject Category:Genetics.
- Copy-number_variation subject Category:Molecular_biology.
- Copy-number_variation comment "Copy-number variations (CNVs)—a form of structural variation—are alterations of the DNA of a genome that results in the cell having an abnormal or, for certain genes, a normal variation in the number of copies of one or more sections of the DNA. CNVs correspond to relatively large regions of the genome that have been deleted (fewer than the normal number) or duplicated (more than the normal number) on certain chromosomes.".
- Copy-number_variation label "Copy-number variation".
- Copy-number_variation label "Copynumbervariaties".
- Copy-number_variation label "Gene copy number variants".
- Copy-number_variation label "Variabilité du nombre de copies".
- Copy-number_variation label "Variación en el número de copias".
- Copy-number_variation label "Вариация числа копий генов".
- Copy-number_variation label "コピー数多型".
- Copy-number_variation sameAs Gene_copy_number_variants.
- Copy-number_variation sameAs Variación_en_el_número_de_copias.
- Copy-number_variation sameAs Variabilité_du_nombre_de_copies.
- Copy-number_variation sameAs コピー数多型.
- Copy-number_variation sameAs 유전자_복제수_변이.
- Copy-number_variation sameAs Copynumbervariaties.
- Copy-number_variation sameAs m.0914l6.
- Copy-number_variation sameAs Q1501491.
- Copy-number_variation sameAs Q1501491.
- Copy-number_variation wasDerivedFrom Copy-number_variation?oldid=606334239.
- Copy-number_variation depiction Gene-duplication.png.
- Copy-number_variation isPrimaryTopicOf Copy-number_variation.