Copy number variation across European populations

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Abstract

Genome analysis provides a powerful approach to test for evidence of genetic variation within and between geographical regions and local populations. Copy number variants which comprise insertions, deletions and duplications of genomic sequence provide one such convenient and informative source. Here, we investigate copy number variants from genome wide scans of single nucleotide polymorphisms in three European population isolates, the island of Vis in Croatia, the islands of Orkney in Scotland and the South Tyrol in Italy. We show that whereas the overall copy number variant frequencies are similar between populations, their distribution is highly specific to the population of origin, a finding which is supported by evidence for increased kinship correlation for specific copy number variants within populations. © 2011 Chen et al.

Figures

  • Figure 1. Geographic distribution of study samples.
  • Table 1. Characteristics of Copy Number Variants (CNVs) in Dalmatian, Orcadian and South Tyrolean populations.
  • Figure 2. Distribution of CNV lengths in the three genetic isolate populations.
  • Table 2. Copy Number Variable Regions (CNVRs) in the three genetic isolate populations.
  • Figure 3. Venn diagram showing the number of CNVR shared between the three European genetic isolate populations.
  • Figure 4. CNVR sharing in Dalmatian, Orcadian and South Tyrolean populations. (a) The population make up for each shared CNVR (shared by at least two individuals): each vertical bar represents for a CNVR, the height of each bar is the number of CNV carriers for each CNVR; colour blocks depict the proportions of CNV carriers from each of the three populations, green = Vis, red = Orkney, blue = South Tyrol. (b) Summary of population presentations for CNVRs of different frequencies: each bar represents a group of CNVRs of a certain frequency (from occurring twice to more than 10 times), different colours indicate the proportion of CNVRs private to only one population (in dark grey), CNVRs present in 2 populations (in grey) and CNVRs present in all 3 populations (in light grey). doi:10.1371/journal.pone.0023087.g004
  • Figure 5. Genetic Clustering of individuals according to CNV genotypes. Cluster membership according to analyses of genotypes at 406 CNVR loci in 1893 individuals, for K = 2, 3 and 4. Each inferred cluster is represented by a different color. Cluster 1, Cluster 2 and Cluster 3 refers to Vis, Orkney and South Tyrol, respectively. doi:10.1371/journal.pone.0023087.g005
  • Figure 6. The schematic distribution of CNVs on all autosomes, in a physical map. The length of each chromosome arm is adjusted to be 100 Mb. Each bar comprises CNVs in a 1 Mbp bin on the chromosomes. doi:10.1371/journal.pone.0023087.g006

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CITATION STYLE

APA

Chen, W., Hayward, C., Wright, A. F., Hicks, A. A., Vitart, V., Knott, S., … Porteous, D. J. (2011). Copy number variation across European populations. PLoS ONE, 6(8). https://doi.org/10.1371/journal.pone.0023087

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