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Diversity of VNTR loci. For each VNTR locus the tandem repeat (TR) copy numbers are given with their respective prevalence in our dataset. VNTR A: 8 alleles (2, 4, 5, 6, 7, 8, 10, 13 TR), VNTR B: 1 allele (6 TR) and no amplicon in 8.2% of the strains (the ERIC II and IV strains), VNTR C: 3 alleles (3, 4, 5 TR), VNTR D: 3 alleles (3, 7, 11 TR), VNTR E: 6 alleles (1, 2, 3, 4, 5, 6) and no amplicon in 0.5% of the strains (ERIC III strains).
