Method of providing the information of gene copy number variation associated with height

摘要

The present invention relates to information of gene copy number variation (CNV). The gene of the present invention is related to the human height and is located close to GPR133 of 12q24.33. In particular, the present invention relates to a marker for the gene copy number variation by deleting the gene copy number of human DNA 12q24.33. The deletion of the gene copy number is characterized by 130363561bp or 130381275bp of deleted chromosome 12. The present invention provides a method of providing the information of gene copy number variation which is made, at 12q24.33 of the human chromosome, by the deletion of the gene copy number and is related to human height.