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Figure 2 | Genome Biology

Figure 2

From: Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes

Figure 2

Map of 15q13-q14 at proximal end of contig NT_010194. This part of the map is an updated version of the same region that we analyzed previously [20], with some differences in segment labeling. RP11 clones representing the two possible haplotypes are arbitrarily placed either above or immediately below the segments, with the non-RP11 clones placed below the contig label. Asterisks indicate representative clones used in the contig. Solid lines indicate completely sequenced clones, and dotted lines indicate draft sequences (high throughput genomic sequences [htgs]). A solid line with a dotted line extension indicates a clone in which only a part has been completely sequenced. A gap in a clone indicates a deletion. kb, kilobases.

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Genome Biology

ISSN: 1474-760X

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