The characteristic of a chromosome would make non homologous recombination more likely to be nonhomologous regions of homologous chromosomes.
Biology uses the term "single nucleotide polymorphism" (SNP) to describe a single base pair variation that is prevalent in the population. A mutation is defined as any change in the DNA sequence. In more detail, a polymorphism is any genomic region where at least two distinct sequences are discovered, with each sequence present in at least 1% of the population. The word "polymorphism" is frequently used to describe a normal variation or one that doesn't directly cause sickness. Additionally, the threshold of at least 1% prevalence for a variation to be categorized as a polymorphism is somewhat arbitrary; if the frequency is lower than this, the allele is often recognized as a mutation.
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