The estimated cumulative genome coverage of Thai
CNVRs was 8.72%, which is similar to an earlier report using
relatively homogeneous study population [8]. In accordance with
HapMap3 study, the majority of Thai CNVs characterized were
at low allele frequency, and the allele frequency spectrum of CNVs
with .10% frequency was relatively similar between the Thai and
HapMap3 populations. However, the larger Thai population
sample size may contribute to the higher absolute number of low
frequency CNVs in the Thai individuals observed