Candidate structural variations identified by complete genome sequencing.

Structural variations such as large deletions, insertions inversions or translocations were predicted using whole genome sequencing data. Structural variations were hypothesized in the presence of a junction sequence: a hybrid sequence composed of two non-adjacent fragment of DNA. In the table are reported the candidate structural variations of this B3 thymoma: the extremity position of the 2 joint sequences and the strand of orientation. Among these candidates only the translocation t(11;X) was confirmed by PCR.