Using genome-wide SNP microarray data from over 100,000 DNA samples in total, two recent studies have provided evidence that clonal mosaicism — the co-existence of cells with two or more distinct karyotypes within an individual — increases with age, demonstrating that our DNA changes in subpopulations of cells over time. Furthermore, these studies also suggest that clonal mosaicism may be a risk factor for cancer and that the identification of such chromosomal abnormalities may be a useful screening tool in the future.