From: A bioinformatics approach for identifying transgene insertion sites using whole genome sequencing data
T-DNA
Event
Mapped chromosome
Insert orientation
Chr.
Accession
Start
End
Deletion
pSRT-Bt9
5
10
AP014966.1
22,498,218
22,498,297
79
3′-5’
30
11
AP014967.1
22,473,585
22,473,636
51
109
3
AP014959.1
N/D
14,707,459–14,707,391
-