Dear Biostars,
Does anyone have a good journal article discussing the factors that determine the length of a structural variant in humans? I ask because I have done a genomewide SV burden analysis in a case-control cohort and have found two genes to have a higher SV burden in cases versus controls. However, in the first gene the signal stems from SVs <10kb, but in the latter gene the signal is from SVs >10kb. I am trying to get my head around the biology that may be at play here and would appreciate a reference!
Note I have ready plenty about SV/CNVs generally but specifically I would like something on what affects their length.
All the best
Many thanks for taking time to reply. Will check these out!