Chromosomal abnormality Reference
Deletion in 1p22.2-p31.1 [35]
Deletion 5p15 (5p15.33-pter) [36-40]
Duplication 10~p14-p15 [41]
Deletion in 12p13.33 [42,43]
Duplication 14q23.1 [44,45]
Deletion 15q24.1  [46,47]
Trisomy 18 [48]
Deletion 22qter  [49]
Deletions 22q11.2  [50-52]
Trisomy 22 [53]
Duplication 22q11.1-q11.21 [54,55]
Partial 22 trisomy of the 22q11 region [56]
X chromosome aneuploidies [57-59]
Translocation t(9;18)(p23;q12.2) [60]
Inversion inv9(p11;q13) [61]
Inversion inv14(p11.2;q22.3)   [62]
Mosaicism of trisomy 7 [63]
Mosaicism of trisomy 9 [64,65]
Mosaicism of trisomy 22 [64]
Table 2: Published Chromosomal anomalies in patients with phenotypic characteristics of OAVS.