Table 1.

Overview of investigated inversions

Case IDAscertainmentKaryotypeGRCh37GRCh38T2TChimpanzeeBonoboSequencing data
RD_P525Repeated IVF without pregnancy46,XY,inv(5)(p13q23)lrGS
P4855_501Neurodevelopmental disorder, hearing loss, visual impairment, anosmia, hypogonadism46,XY,inv(6)(p12q16.3)×srGSa, lirGSa, lrGS
P5371_208Recurrent miscarriages46,XY,inv(9)(p13q22)×××××srGSa, lirGSa
BH16643-1Hypotonia, global developmental delay46,XX,inv(9)(q12q34.3)dn××××srGS, lrGS, OGM
P4855_106Family investigation46,XY,inv(10)(q11q23)pat××××srGSa, lirGSa
P4855_208Neurodevelopmental disorder46,XY,inv(11)(p11.1q12)mat×××××srGSa, lirGSa, lrGS
RD_P541Recurrent miscarriages46,XX,inv(12)(p11.23q13.3)lrGS, OGM
RD_P549Family investigation46,XY,inv(14)(q24q32)lrGS
P5370_201Diabetes type II, Hodgkins lymphoma, hearing loss, hypogonadism, retinitis pigmentosa, acanthosis nigricans, beta thalassemia46,XY,inv(18)(p11.3q11.2)×××××srGSa, lirGSa
RD_P526Family investigation46,XX,inv(18)(p11.23q21.1)lrGS
RD_P542Repeated IVF without pregnancy46,XX,inv(19)(p13.2q13.4)lrGS
RD_P546Family investigation46,XY,inv(19)(p13.2?q13.4)lrGS

[i] 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]).

[ii] aPreviously reported in Pettersson et al. (2020).