Nazarenko S A, Puzyrev V P
Hum Genet. 1985;71(2):100-2. doi: 10.1007/BF00283361.
A cytogenetic study of Khanty from the lower Ob river in West Siberia has detected a high frequency of the Y chromosome heterochromatin subtotal deletion--del(Y)(q12). This morphologically identical deletion was found in 32 of 154 males examined (20.8%). The carriers had 10 different surnames. Taking into account the small size, isolation by distance, and historical peculiarities of the surname formation of the population, it has been concluded that the high frequency of the del(Y)(q12) results from the genetic drift of the marker chromosome.
对西西伯利亚鄂毕河下游汉特人的细胞遗传学研究发现,Y染色体异染色质部分缺失——del(Y)(q12)的频率很高。在154名接受检查的男性中有32人(20.8%)发现了这种形态相同的缺失。携带者有10个不同的姓氏。考虑到该人群姓氏形成的群体规模小、距离隔离和历史特殊性,得出结论:del(Y)(q12)的高频率是由标记染色体的遗传漂变导致的。