Table 3.

Features of rearrangements and breakpoints

HaplotypeRearrangementNAHR SD pairBreakpoint
ClassSize (bp)Length (kbp)Identity (%)Length (bp)Identity (%)GenesRepetitive elementsGC content (%)
H2.1Inversion1,433,44844699.4617,42099.80NPY4RLarge region49
H2.2Inversion1,321,41444699.46499399.64AC244230.2Large region48
H2.3Inversion1,510,97444699.46499999.84LINC00842Large region52
H2.4Inversion993,56844699.4625,59899.89AL136982.3Large region39
H2.5Inversion902,23044699.46722099.74FAM245BLarge region36
H3Deletion176,4061894.36369100NoNo66
H5Duplication714,5245699.15867100NoLINE L1M443
H9Inversion1,089,2326899.201207100ANXA8LINE L4_C_Mam51
H10Deletion501,66744699.4619,95799.79FAM245BLarge region34
H11Deletion671,79612299.63164199.70FRMPD2LTR33 + MER2052

[i] The length and identity of the entire SD pair mediating the NAHR event as well as features of the narrowed breakpoint sequence are shown. Data were taken from the CAT + Liftoff Gene Annotations, RepeatMasker Repetitive Elements, and GC Percent in 5-Base Windows UCSC Genome Browser tracks (T2T-CHM13 v2.0).