Table 2.

Characteristics of the resolved breakpoint junctions (BPJs) of marker and ring chromosomes, with coordinates mapped to the T2T-CHM13v2.0 genome build

Case IDsSMCBPJChrPosAPosBSegment posA–posBPosA: genesPosB: genesPosA: repeatPosA: segmental duplicationPosB: segmental duplicationPosB:

repeat
Microhomology (bp)Insertion (bp)Mechanism
RD_P276r(5)1Chr 537,676,10343,290,183A–BWDR70, intron 5AC025171.1, intron 2LTR:MLT1H2Cent.3MMEJ
2Chr 532,320,80949,497,791aA–BLTR:MLT1F2Cent.3
RD_P278r(7)1Chr 759,987,27472,094,570A–BCent.YesAluSx120 NTMMBIR
2Chr 759,978,28159,987,351A–BCent.YesYesCent.3
RD_P273r(8)1Chr 850,587,59577,860,383A–BSNTG1AC062004.1L1P12MMEJ
2Chr 846,120,188a51,426,338A–BCent.4 (templated)
RD_P272r(9)1Chr 930,592,55731,057,050B–CL2c, L2a28 NTMMBIR
2Chr 928,144,04331,568,556A–CLINGO2, intron3L2d2L1P1224 NT
3Chr 929,574,52491,174,804A–FAluSx13
4Chr 939,306,74791,060,755D–FAluYk2, SatelliteYesMIRc
5Chr 932,076,51244,448,128D–EANKRD20A7P (pseudogene)L1PB3YesCent.100 NT
RD_P166r(13)1Chr 1311,452,84056,358,138A–CPRR20C, intron 1Cent.YesYes42 (templated)MMBIR
2Chr 1329,045,86784,773,620B–CUBL3, intron 1LINC00351, intron 1AluSp
RD_P550r(14)1Chr 149,208,60416,434,843A–AAC244502.1, TRACent.YesCent., LTR/ERV12MMEJ
RD_P275r(20)1Chr 204,979,43459,369,410A–CSLC23A2, intron 2LOC102724968L2205 (templated)MMBIR
2Chr 2024,892,35565,776,662B–CUCKL1, intron 1Cent.7b2b
3Chr 203,306,02042,368,945A–BDNAAF9/C20orf194/MSTRG4
RD_P328der(7)t(X;7;5)1Chr 7-Chr 5Chr 7: 43,886,314Chr 5: 177,119,928A–BCOA1, intron 1CDHR2, exon 9L1MB8, AluYk2MMEJ
2Chr X-Chr7Chr X: 14,614,119Chr 7: 75,313,264C–ALIMK1, intron 10Simple repeats (AAAT)AluJb3
RD_P586der(X)1Chr X103,977,823145,148,123F–JIL1RAPL2, intron 6L2d, L1M4a1L1MA11MMBIR
2Chr X89,566,57289,651,697F–EL1ME1YesL1ME3, ERVL-MaLR
3Chr X66,181,02884,675,390B–EDACH2, intron 1L1ME3B2
4Chr X58,080,09866,184,481A–BNANALINE/L2a2
5Chr X74,310,915144,750,571A–HL1PA7, MLT2D, L1MEcL1MA2, ERVL-MaLR1
6Chr X83,792,179141,176,418D–HPOF1B, intron 3L1PREC237 NT (L1)
7Chr X75,059,48683,829,717C–DL1PBaL1MEd, L1MA129 NT
8Chr X83,190,23391,038,187D–GTEX16P (pseudogene)PCDH11X, intron 5Yes41 NT
9Chr X91,089,607144,762,724G–IL1MB7, L1PBb, L1PA13YesLTR16B133 NT

[i] (Chr) Chromosome; (Pos) position; (bp) base pairs; (NT) nontemplated; (NA) not applicable; (MMBIR) microhomology-mediated break-induced replication; (MMEJ) microhomology-mediated end joining.

[ii] Positions marked in bold indicate the breakpoint in sequence is not present in GRCh38 (Bilgrav Saether et al. 2024). The size of each segment is available in Supplemental Table S2.

[iii] aAmbiguous position.

[iv] bComplex mechanism.