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. 2020 Sep 16;58(11):783–788. doi: 10.1136/jmedgenet-2020-106909

Table 1.

Segregation of pericentromeric STSs

Marker Chr Cytoband Distance from cen (bp) II-7 III-12 III-15 II-8 MI MII
D4S405 4 4p14 9 307 605 bc bbb* acc ab III-15
D4S428 4 4q12 2 974 289 ab aab aab bb III-12 and III-15
D5S418 5 5p13.1 6 389 874 bc NA acc ad III-15
D5S1969 5 5q11.2 3 837 191 bc NA bbd ad III-15
D6S257 6 6p12.1 2 911 729 bc NA bbd ad III-15
D8S532 8 8p11.21 3 050 515 bd NA abb ac III-15
D12S1663 12 12q12 6 414 865 bb bbc bbc ac
D13S175 13 13q12.11 1 848 380 ac NA ccd bd III-15
D15S128 15 15q11.2 5 130 705 bc acc abb ac III-15
D19S414 19 19q12 4 232 942 ab bbd bbd cd III-12 and III-15
D19S566 19 19p13.11 5 519 801 bc ccd abb ad III-12 and III-15
DXS991 X Xp11.21 3 112 973 aa NA aab bb

STS alleles are indicated for each individual by a letter with ‘a’ being the largest amplicon. Alleles are underlined if maternal origin is evident. The last two columns indicate if triploidy appears to be originated from meiosis I (MI) or meiosis II (MII).

*Only one type of allele is evident.

mat, maternal; NA, not assessed; STS, sequence-tagged site.