Table 2.
BAC Clone | WVI | GGA/TGU | Orientation | Rearrangements |
---|---|---|---|---|
CH261-119K2 | 1a | 1 | 1 | Fusion |
CH261-83O13 | 1a | 1 | 2 | Fusion |
CH261-36B5 | 1a | 1 | 3 | Fusion |
CH261-118M1 | 1 | 1 | 4 | Inversion |
CH261-168O17 | 1 | 1 | 8 | Inversion |
CH261-107E2 | 1 | 1 | 7 | Inversion |
CH261-58K12 | 1 | 1 | 6 | Inversion |
CH261-184E5 | 1 | 1 | 5 | Inversion |
TGMCBA-340P4 | 3 | 2 | 1 | Inversion |
CH261-169N6 | 3 | 2 | 2 | Inversion |
CH261-50C15 | 3 | 2 | 4 | Inversion |
TGMCBA-78C11 | 3 | 2 | 3 | Inversion |
CH261-44D16 | 3a | 2 | 5 | Inversion |
TGMCBA-295P5 | 2 | 3 | 1 | Fusion |
TGMCBA-130M12 | 2 | 3 | 3 | Inversion |
CH261-160I6 | 2 | 3 | 4 | Inversion |
CH261-97P20 | 2 | 3 | 5 | Inversion |
CH261-17B14 | 2 | 3 | 6 | Inversion |
CH26-250J17 | 2 | 3 | 2 | Inversion or translocation |
TGMCBA-64D9 | 2 | 3 | 7 | Inversion |
CH261-120H23 | 2 | 3 | 8 | Fusion |
TGMCBA-330J11 | 4a | 4 | 2 | Inversion |
CH261-111A15 | 4a | 4 | 1 | Inversion |
CH261-18C6 | 4 | 4 | 3 | Inversion |
CH261-85H10 | 4 | 4 | 4 | Inversion |
CH261-89P6 | 4 | 4 | 5 | Fusion |
TGMCBA-216A16 | 4 | 4 | 6 | Fusion |
CH261-73F2 | 6 | 5 | 1 | Inversion |
CH261-49B22 | 6 | 5 | 3 | Inversion |
CH261-122F8 | 9* | 5 | 4 | Inversion |
CH261-78F13 | 9* | 5 | 2 | Inversion |
TGMCBA-382J4 | 5 | 6 | 2 | Inversion |
CH261-49F3 | 5 | 6 | 1 | Inversion |
CH261-56K7 | 7 | 7 | 1 | Fusion |
TGMCBA-34L13 | 7 | 7 | 2 | Inversion |
CH261-186K14 | 7 | 7 | 3 | Inversion |
CH261-38E18 | 7 | 7 | 4 | Fusion |
TGMCBA-252A4 | 10 | 8 | 1 | Inversion |
CH261-187M16 | 8 | 9 | 1 | Fusion |
CH261-42P16 | 6p distal | 17 | 2 | Fusion |
TGMCBA-375I5 | 6p distal | 17 | 1 | Fusion |
TGMCBA-200J22 | Z | Z | 1 | Fusion |
TGMCBA-270I9 | Z | Z | 2 | Fusion |
*Probes overlapped in the fish images **The correct position of the micro involved is beyond the scope of this paper due to the absence of the WVI genome; The BACs used are those previously developed by Damas et al. [25]. The orientation means the order of the BAC clone in WVI karyotype