In this study, a total of 191 cases with STR exclusions out of 591 paternit
y cases were analysed using 2 STR sets, i.e. (set a) 5 STRs in 462 cases wi
th 150 exclusions and (set b) 9 STRs in 129 cases with 41 exclusions. Set (
a) was associated with four exclusions on average while set (b) showed five
exclusionary loci on average. Double exclusions were observed in Is cases
and further elaborated. Of these, 2 ended up with probabilities of paternit
y of 0.1% and 0.4%, respectively and with a random occurrence of the hypoth
esis "mutation" of 1:20,000 and 1:50,000, respectively, while all other cas
es were associated with much lower frequencies. The conclusion is that the
evidential value of a set of highly polymorphic STRs applied in paternity c
ases is usually extremely high.