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Table 2 Linear regression analyses summarizing the significant relationship of ChrY CNV with EAE susceptibility and phenotypes associated with X-Y intragenomic conflict

From: Copy number variation in Y chromosome multicopy genes is linked to a paternal parent-of-origin effect on CNS autoimmune disease in female offspring

X

Female CDS

Male CDS

Sex ratio

Sperm head abnormalities

Sly

F = 17.66; P = 0.0012

F = 13.26; P = 0.0034

F = 82.03; P < 0.0001

F = 19.65; P = 0.0016

Ssty1

F = 7.442; P = 0.0183

F = 12.31; P = 0.0043

F = 8.452; P = 0.0131

F = 9.173; P = 0.0143

Ssty2

F = 0.4947; P = 0.4953

F = 6.323; P = 0.0272

F = 0.1788; P = 0.6798

F = 0.8289; P = 0.3863

Srsy

F = 5.958; P = 0.0311

F = 0.5336; P = 0.4791

F = 9.191; P = 0.0104

F = 14.38; P = 0.0043

Rbmy

F = 9.378; P = 0.0099

F = 8.751; P = 0.012

F = 23.95; P = 0.0004

F = 8.535; P = 0.017

Rbm31y

F = 3.017; P = 0.108

F = 2.156; P = 0.1677

F = 11.14; P = 0.0059

F = 3.024; P = 0.116