Table 1.
Case ID | Ascertainment | Karyotype | GRCh37 | GRCh38 | T2T | Chimpanzee | Bonobo | Sequencing data |
---|---|---|---|---|---|---|---|---|
RD_P525 | Repeated IVF without pregnancy | 46,XY,inv(5)(p13q23) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS |
P4855_501 | Neurodevelopmental disorder, hearing loss, visual impairment, anosmia, hypogonadism | 46,XY,inv(6)(p12q16.3) | × | ✓ | ✓ | ✓ | ✓ | srGSa, lirGSa, lrGS |
P5371_208 | Recurrent miscarriages | 46,XY,inv(9)(p13q22) | × | × | × | × | × | srGSa, lirGSa |
BH16643-1 | Hypotonia, global developmental delay | 46,XX,inv(9)(q12q34.3)dn | × | × | ✓ | × | × | srGS, lrGS, OGM |
P4855_106 | Family investigation | 46,XY,inv(10)(q11q23)pat | × | × | ✓ | × | × | srGSa, lirGSa |
P4855_208 | Neurodevelopmental disorder | 46,XY,inv(11)(p11.1q12)mat | × | × | × | × | × | srGSa, lirGSa, lrGS |
RD_P541 | Recurrent miscarriages | 46,XX,inv(12)(p11.23q13.3) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS, OGM |
RD_P549 | Family investigation | 46,XY,inv(14)(q24q32) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS |
P5370_201 | Diabetes type II, Hodgkins lymphoma, hearing loss, hypogonadism, retinitis pigmentosa, acanthosis nigricans, beta thalassemia | 46,XY,inv(18)(p11.3q11.2) | × | × | × | × | × | srGSa, lirGSa |
RD_P526 | Family investigation | 46,XX,inv(18)(p11.23q21.1) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS |
RD_P542 | Repeated IVF without pregnancy | 46,XX,inv(19)(p13.2q13.4) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS |
RD_P546 | Family investigation | 46,XY,inv(19)(p13.2?q13.4) | ✓ | ✓ | ✓ | ✓ | ✓ | lrGS |
The table displays the reference genome in which the inversion breakpoint junctions were mapped (✓) or absent (×), and the data available (short-read [sr], linked-read [lir], long-read [lr] genome sequencing [GS], and optical genome mapping [OGM]).
aPreviously reported in Pettersson et al. (2020).